510(k) K162951

TUBETECH IV Administration Set by Douglas Medical Products, Inc. — Product Code FPA

K162951 is an FDA 510(k) premarket notification submitted by Douglas Medical Products, Inc. for the device "TUBETECH IV Administration Set". The FDA issued a decision of Substantially Equivalent on July 28, 2017. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Douglas Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 28, 2017
Date Received
October 24, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Administration, Intravascular
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type